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Trials / Completed

CompletedNCT06180200

Study of the in Vivo Expression of MU Opioid Receptors Using PET and the Selective Tracer [C-11] Carfentanil in Normal Weight and Obese Subjects

Status
Completed
Phase
Study type
Observational
Enrollment
16 (actual)
Sponsor
IRCCS San Raffaele · Academic / Other
Sex
Male
Age
18 Years – 40 Years
Healthy volunteers

Summary

Positron emission tomography (PET) is a nuclear medicine technique that allows the measurement, in vivo in humans, with a non-invasive method, of the regional distribution of substances marked with positron emission isotopes such as C-11, in different districts bodily. Using this method it is therefore possible to directly measure at the level of the brain the distribution of receptors, enzymes, reuptake sites, as well as their interaction with various classes of drugs and the related modifications that may be present during the pathology. The evaluation of the endogenous opiate receptor system will be implemented by comparing the in vivo binding maps of 11C carfentanil in the two groups of subjects under examination (normal weight, NOR and obese, OB, based on body mass index, BMI); in fact, experimental data deriving from previous studies support the hypothesis that the basis of obesity and incorrect eating behaviors is a dysregulation of the endogenous ligand-mu opioid receptor interaction. The comparison of the data deriving from the analysis of the PET exams performed on the two groups of subjects will therefore allow us to evaluate the alterations of the opioid system possibly present in obese subjects.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTPET for the analysis of mu opioid receptor expression.PET for the analysis of the expression of mu opioid receptors and to directly measure the distribution of the receptors and enzyme reuptake sites at the brain level.

Timeline

Start date
2004-10-22
Primary completion
2007-12-01
Completion
2007-12-01
First posted
2023-12-22
Last updated
2024-03-06

Source: ClinicalTrials.gov record NCT06180200. Inclusion in this directory is not an endorsement.